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A 36-week Open-label Extension Study of CACZ885H2361 on the Safety and Tolerability of Canakinumab 150 mg s.c. Pre-filled Syringe (PFS) in Treating Acute Gouty Arthritis Flares in Frequently Flaring Patients

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City:   Roseville
State:   California
Zip Code:   95661
Conditions:   Acute Gouty Arthritis
Purpose:   This is a 36 week open-label extension of the canakinumab pre-filled syringe study for safety and tolerability in patients who have frequent flares of acute gouty arthritis.
Study Summary:  
Criteria:   Inclusion criteria: - Compliance and completion of the canakinumab PFS core study - Unchanged significant clinical medical history from entry into core study Exclusion criteria: - Physician judgment of unsuitability for the study - Pregnant or nursing women Other protocol-defined inclusion/exclusion criteria may apply
NCT ID:   NCT01431638
Primary Contact:   Study Director
Novartis Pharmaceticals
Novartis Pharmaceuticals

Novartis Pharmaceuticals
Phone: 862-778-8300
Backup Contact:   N/A
Location Contact:   Roseville, California 95661
United States

Novartis Pharmaceuticals
Phone: 862-778-8300

Site Status: Recruiting

Data Source:   ClinicalTrials.gov
Date Processed:   June 19, 2013
Modifications to this listing:   Only selected fields are shown, please use the link below to view all information about this clinical trial.
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